Product Details

SNP ID
rs140398365
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:89433260 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCAAAGCCAAGCAACACAGAACTA[A/G]ATATCATTGAAAATCCACAGAGGAG
Phenotype
MIM: 611910
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC16A12 PubMed Links

Gene Details

Gene
SLC16A12
Gene Name
solute carrier family 16 member 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_213606.3 1544 Missense Mutation TCT,TTT S452F NP_998771.3
XM_017016237.1 1544 Missense Mutation TCT,TTT S452F XP_016871726.1
XM_017016238.1 1544 Missense Mutation TCT,TTT S452F XP_016871727.1
XM_017016239.1 1544 Missense Mutation TCT,TTT S452F XP_016871728.1

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